EP0007705A1

EP0007705A1 - Modified aminoplast condensation products and process for their preparation

Info

Publication number: EP0007705A1
Application number: EP79301213A
Authority: EP
Inventors: Raymond William Yates
Original assignee: British Industrial Plastics Ltd
Current assignee: British Industrial Plastics Ltd
Priority date: 1978-06-24
Filing date: 1979-06-22
Publication date: 1980-02-06
Also published as: DE2964799D1; NO792100L; AU4828879A; US4250069A; ZA793009B; EP0007705B1; JPS555984A; AU526833B2; FI791985A

Abstract

Improved resins are obtained by substituting urea for part of the melamine in known cationic water-soluble resins obtained by interaction of melamine, an aliphatic hydroxymonoamine such as triethanolamine, and formaldehyde. The new resins, which have molar ratios melamine : urea : hydroxyamine : formaldehyde in the range 1: 0.25-8:0.1-2.5: 4-30, have a faster curing rate and better stability in the liquid state for a given content of formaldehyde.

Description

This invention relates to the preparation of melamine-formaldehyde condensation products, and particularly such products as are modified with aliphatic hydroxymonoamines.
Examples of such modified melamine-formaldehyde condensation products are disclosed in the specifications of our UK Patents 1 305 187 and 1 317 774.
There are described in Specification 1 305 187 certain cationic water-soluble melamine-formaldehyde resins modified with an aliphatic hydroxymonoamine which are specially useful for imparting wet-strength to paper. These resins are obtainable by a two-stage process carried out in aqueous medium, both stages being operated with control of pH. In the process, the molar ratio melamine: formaldehyde employed is in the range 1:2 - 1:6 and the solids content of the system is at least 60% by weight. By this we mean that weight of reactants/(weight of reactants + aqueous medium) is at least 60%.
In Specification 1 317 774 there are described certain cationic water-soluble melamine-formaldehyde resins modified with an aliphatic hydroxymonoamine which are different from those of Specification 1 305 187 in being 'high formaldehyde' resins (they have a molar ratio formaldehyde : melamine greater than 6:1). These resins are useful in anchoring moisture-proof coatings to regenerated cellulose film.
The aliphatic hydroxymonoamine exployed in forming the resins described above are of the general formula ^R _IR₂N-R-OH where

_R is lower alkylene (preferably (CH₂)₂ or (CH2)3)
R₁ is hydrogen, a lower alkyl group (preferably
CH₃ or C₂H₅) or a hydroxy lower alkyl group (preferably (CH₂)₂OH or (CH₂)₃0H), and
R₂ is a lower alkyl group (preferably CH₃ or C₂H₅) or a hydroxy lower alkyl group (preferably (CH₂)₂0H or (CH₂)₃0H).

Examples of such aliphatic hydroxymonoamines are: triethanolamine, tri-n-propanolamine, diethylaminoethanol and dimethylaminoethanol.
We have now found that, by substituting urea for part of the melamine employed in the production of hydroxymonoamine- modified melamine-formaldehyde resins, there can be obtained new resins of faster curing rate and improved stability in the liquid state for a given content of formaldehyde. Additionally, when employed so as to modify the kind of resin described in UK Specification 1 305 187, the substitution results in resins which develop wet strength in paper relatively quickly at ordinary temperature and humidity, a property which is specially useful when manufacturing tissue and towelling on high speed machines.
The new resins are condensates of melamine, urea, an aliphatic hydroxymonoamine and formaldehyde in the following molar proportions:
and with a molar ratio formaldehyde: each amino-hydrogen atom in the range 0.5-2.25 : 1. (Melamine, C₃N₃(NH₂)₃ has 6 amino-hydrogen atoms; and urea, CO(NH₂)₂, has 4 amino-hydrogen atoms.)
In preparing resins suitable for use in paper treatment, the molar ratio melamine: formaldehyde employed is in the range 4-24, with a molar ratio formaldehyde: each amino-hydrogen atom in the range 0.5-1.25: 1. Preferred proportions for such resins are:
In preparing resins of molar ratio formaldehyde: each amino-hydrogen atom in the range 1.25-2.25 : 1, preferred proportions of the constituent substances are:
Those resins having a molar ratio formaldehyde: each amino-hydrogen atom in the range 0.5-1.25 : 1 can be made starting from reaction products of an aliphatic hydroxymonoamine with formaldehyde, which are prepared as described in Specification 1 305 187: that is to say by reacting formaldehyde and hydroxymonoamine in aqueous medium, at a solids content of at least 60% by weight and at pH at least 8.5 (preferably 8.5-11), at a temperature in the range 80^o _C- reflux temperature. Such a product is then reacted with melamine and urea, at least the final stage of the reaction being carried out at reduced pH in the range 6.5-8.5, and preferably 7-7.5. The pH can be reduced by addition of a suitable acid, for example sulphuric, hydrochloric, orthophosphoric, formic or toluene p-sulphonic. The reaction is carried out at a temperature in the range 60°C-reflux temperature, and preferably at 85-95°C, preferably until the viscosity of the system, measured at 30% solids, is 50-400 centipoise (= 0.05-0.4 Pascal seconds) at 25⁰C and preferably 100-200 centipoise (= 0.1-0.2 Pa s). The reaction product can then be diluted with enough water to make it readily pourable at ambient temperature, and then cooled to that temperature. The pH can if necessary be adjusted by addition of acid or hydroxymonoamine to a value in the range 6.5-7.5, and the product can be set aside for storage.
In the procedure just described, it is convenient to start with the hydroxymonoamine alone, using at that stage enough' formaldehyde not only to react with the hydroxymonoamine but also to provide for the subsequent addition reactions with melamine and urea.
In alternative procedures, the melamine and urea can be included, together or separately, in the first stage with formaldehyde and amine, or can be used initially to produce a reaction product with formaldehyde before the hydroxymonoamine is introduced.
In making those resins having a molar ratio formaldehyde: each amino-hydrogen atom in the range 1.25-2.25 : 1, the procedure can follow generally that described for the resins of lower formaldehyde content, but there is no need to provide for a solids content of at least 60% by weight; and this is so whether the 'extra' formaldehyde is added at the first stage or (as in Example 6 later) at the last.
The invention is further illustrated by the following Examples, which relate to the preparation of storage-stable cationic resins miscible with water in all proportions
at 25⁰C. Examples 1-5 relate to resins of free formaldehyde content not greater than 6% by weight at 30% solids concentration, and Example 6 to a high formaldehyde content resin, with free formaldehyde greater than 10% by weight at 50% solids concentration.

Example 1-

328.6g (9.96 moles) of 91% formaldehyde, 204.6g (2.45 moles) of 36% formalin and 344g (2.97 moles) of 90% triethanolamine were charged to a reactor flask and the mixture (pH=₁₀.₅) was heated to 85⁰C. This temperature was maintained for 2 hours, and the mixture was then cooled to 50°C. 130.7g (1.03 moles) of melamine, 130.7g (2.17 moles) of urea and 312g of water were then added and the temperature was raised to 60°C. At this point heating was stopped and the exothermic reaction in progress was allowed to subside. The mixture was then adjusted to pH 7.1 (glass electrode at 25°C) by the addition of 70ml of 90% formic acid and heating was restarted to maintain a temperature of 85-90°C until the viscosity had, as a. result of the condensation reaction, risen to 8Pa s (at 25°C). 1100g of water were then added (solids content was then 28.5%) and the resin was cooled immediately to 25°C. Its viscosity was 58.4centipoise (0.06Pa s) at 25°C.

Examples 2, 3 and 4

The procedure of Example 1 was followed generally, but with the following differences in detail:

Example 5

316.8g (9.6 moles) of 91% formaldehyde, 197.2g (2.36 moles) of 36% formaldehyde and 82.9g (0.5 moles) of 90% triethanolamine were charged to a reactor flask and heated at 85-90°C for 2 hours. After cooling to 50°C, 63g (0.5 moles) of melamine, 216g (3.6 moles) of urea and 220.8g of water were added and the mixture was heated to 60°C. When the exothermic reaction had subsided, the mixture was brought to pH 7 by addition of 18ml of 90% formic acid. The mixture was heated at 85-90°C and, when its viscosity (measured at 25°C) had risen to 8Pa s, water (731.2g) was added. The syrupy resin was finally cooled to room temperature.

Example 6

1000g (12 moles) of 36% formaldehyde and 332g (2 moles) of 90% triethanolamine were charged to a reactor flask and heated at 85-90°C for 2 hours. After cooling to 50°C, 12Gg (1 mole) of melamine and 126g (2.1 moles) of urea were then added, and the mixture was heated to 60°C. When the exothermic reaction had subsided, 60ml of 90% formic acid were added to bring the syrup to pH 7.3. The mixture was heated at 85-90°C until the viscosit (measured at 25°C) had risen to 2-4Pa s, and 320g of water were then added. Heating at 85-90°C was then continued until the viscosity (at 25°C) reached 6Pa s. 528g (16 moles) of 91% formaldehyde were added, and heating at 85-90°C was continued (15 mins) until only a single liquid phase was present, and then for a further 15 minutes. The syrupy resin was rapidly cooled to 30°C and then adjusted to pH 7 with 90% formic acid. Its solids content was 48.3%. by weight.

Testing of product

The resin prepared according to Example 1 was evaluated for wet-strength performance in comparison with a resin prepared identically except for the replacement of the urea by an equal weight of melamine. Hand sheets were prepared on a standard form of apparatus (British Pulp and Board Makers Association) using bleached sulphite pulp beaten to a freeness of 32° Schopper-Reigler. In each case the equivalent of 2 parts by weight of solid resin per 100 parts of bone-dry pulp was used, the pulp suspension and backwater system being adjusted to pH 5.5 with dilute hydrochloric acid. Of the hand sheets so produced, some were cured at 85°C and some were allowed to age naturally at 65°F and 50% RH (relative humidity). Wet-strength values, expressed as breaking length (metres) of 15mm wide strips, wei
These results show faster development of wet-strength with the use of the melamine-urea-hydroxyamine-formaldehyd₄ condensate than with the use of the melamine-hydroxyamine-formaldehyde condensate.

Claims

1. A cationic water-soluble melamine-urea-aliphatic hydroxymonoamine-formaldehyde resin having molar ratios melamine: urea: hydroxymonoamine: formaldehyde in the ranges 1 : 0.25-8 : 0.1-2.5 : 4-30 and a molar ratio formaldehyde: each amino-hydrogen atom in the range 0.5-2.25 : 1.

2. A cationic water soluble resin according to Claim 1, in which the molar ratios melamine: urea: aliphatic hydroxymonoamine: formaldehyde are 1 : 0.25-8 : 0.1-2.5 : 4-24 and the molar ratio formaldehyde: each amino hydrogen atom is 0.5-1.25 : 1.

3. A cationic water-soluble resin according to Claim 2, in which the molar ratios melamine : urea : aliphatic hydroxymonoamine : formaldehyde are 1 : 1.5-3.5 : 0.5-2 : 10-15.

4. A cationic water-soluble resin according to Claim 1, in which the molar ratios melamine : urea : aliphatic hydroxymonoamine : formaldehyde are 1 : 1.5-3.5 : 0.5-2 : 10-30 and the molar ratio formaldehyde: each amino-hydrogen atom is in the range 1.25-2.25 : 1.

5. A cationic water-soluble resin according to Claim 4, in which the molar ratio melamine : formaldehyde is in the range 1 : 16-28.

6. A cationic water-soluble resin according to any one of Claims 1 to 5, derived from an aliphatic hydroxymonoamine which is a tertiary amine.

7. A cationic water-soluble resin according to Claim 6, in which said amine is a tri-(lower alkanol) amine.

8. A cationic water-soluble resin according to Claim 7, in which the tri-(lower alkanol) amine is triethanoaminc.

9. A method of making a resin as set forth in Claim 1, in which the product obtained by reacting formaldehyde and an aliphatic hydroxymonoarnine at elevated temperature in an aqueous medium of pH at least 8.5 and solids content at least 60% is reacted with melamine and urea at elevated temperature, at least the final stage of the latter reaction being carried out at reduced pH in the range 6.5-8.5.

10. A method according to Claim 9, in which said reduced pH is in the range 7-7.5.

11. A method according to Claim 9 or 10, in which the reaction with melamine and urea at pH in the range 6.5-8.5 is carried out until the viscosity of the system, measured at 30% solids content and 25°C, is in the range 0.05-0.4 Pascal seconds.

12. A method according to Claim 11, in which said viscosity is in the range 0.1-0.2 Pascal seconds.

13. A method of making a resin as set forth in Claim 4, in which the product obtained by reacting formaldehyde and an aliphatic hydroxymonoamine at elevated temperature in an aqueous medium of pH at least 8.5 is reacted with melamine and urea at elvated temperature, at least the final stage of the latter reaction being carried out at reduced pH in the range 6.5-8.5; and the melamine-urea-hydroxyamine-formaldehyde product so formed is reacted with further formaldehyde to obtain a product of molar ratio formaldehyde: each amino-hydrogen atom in the range 1.25-2.25 : 1.

14. A cationic water-soluble melamine-urea-aliphatic hydroxymonoamine-formaldehyde resin substantially as described with reference to Examples 1 to 5.

15. A cationic water-soluble melamine-urea-aliphatic hydroxymonoamine-formaldehyde resin substantially as described with reference to Example 6.

16. A cationic water-soluble melamine-urea-aliphatic hydroxymonoamine-formaldehyde resin whenever obtained by the method of any one of Claims 9-13.